Shopping Cart
  • Remove All
  • TargetMol
    Your shopping cart is currently empty
Filter
Applied FilterClear all
TargetMol | Tags By Target
  • HSV
    (10)
  • DNA/RNA Synthesis
    (5)
  • HCV Protease
    (4)
  • Nucleoside Antimetabolite/Analog
    (4)
  • Antiviral
    (3)
  • Influenza Virus
    (3)
  • Antifection
    (2)
  • Apoptosis
    (2)
  • CDK
    (2)
  • Others
    (27)
Filter
Search Result
Results for "

cytomegalovirus

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    50
    TargetMol | Inhibitors_Agonists
  • Compound Libraries
    1
    TargetMol | Compound_Libraries
  • Peptide Products
    5
    TargetMol | Peptide_Products
  • Inhibitory Antibodies
    3
    TargetMol | Inhibitory_Antibodies
  • Natural Products
    3
    TargetMol | Natural_Products
  • Recombinant Protein
    16
    TargetMol | Recombinant_Protein
  • Isotope Products
    1
    TargetMol | Isotope_Products
  • Antibody Products
    4
    TargetMol | Antibody_Products
SIRT1-IN-1
T9648352554-02-0In house
SIRT1-IN-1 is a selective inhibitor of SIRT1 with an IC50 of 205 nM. SIRT1-IN-1 is an inhibitor of cytomegalovirus (CMV) with antiviral activity.
  • Inquiry Price
Size
QTY
Ganciclovir
RS-21592, BW 759, 2'-Nor-2'-deoxyguanosine
T068882410-32-0
Ganciclovir (2'-Nor-2'-deoxyguanosine) is an ACYCLOVIR analog that is a potent inhibitor of the Herpesvirus family including cytomegalovirus. Ganciclovir is used to treat complications from AIDS-associated cytomegalovirus infections.
  • Inquiry Price
Size
QTY
Floxuridine
NSC 27640, FUDR, Deoxyfluorouridine, 5-Fluorouracil 2'-deoxyriboside
T096450-91-9
Floxuridine (FUDR) is an antimetabolite, floxuridine inhibits thymidylate synthase, resulting in disruption of DNA synthesis and cytotoxicity.
  • Inquiry Price
Size
QTY
Xanthohumol
T33426754-58-1
Xanthohumol, also known as 2', 4, 4'-trihydroxy-6'-methoxy-3'-prenylchalcone or desmethylxanthohumol, is a member of the class of compounds known as 3-prenylated chalcones. It inhibits COX-1 and COX-2 activity and shows chemopreventive effects.
  • Inquiry Price
Size
QTY
Cidofovir
HPMPC, GS 0504, (S)-HPMPC
T6244113852-37-2
Cidofovir ((S)-HPMPC) inhibits virus replication by specific inhibition of viral DNA synthesis.
  • Inquiry Price
Size
QTY
Bisindolylmaleimide IV
T7659119139-23-0
Bisindolylmaleimide IV is a protein kinase C (PKC) cell permeable inhibitor( IC50 : 0.10 - 0.55 μM)
  • Inquiry Price
Size
QTY
Valganciclovir hydrochloride
Valganciclovir HCl, Valcyte, Valcyt
T1533175865-59-5
Valganciclovir hydrochloride (Valganciclovir HCl) is a hydrochloride salt form of valganciclovir, a prodrug form of ganciclovir, a nucleoside analog of 2'-deoxyguanosine, with antiviral activity. After phosphorylation, valganciclovir is incorporated into DNA, resulting in inhibition of viral DNA polymerase, and viral replication.
  • Inquiry Price
Size
QTY
B220
T10445112228-65-6In house
B220, an antiviral agent, inhibits the growth of HSV-1, HSV-2, and human cytomegalovirus (CMV).
  • Inquiry Price
6-8 weeks
Size
QTY
BAY-43-9695
T67788233255-39-5In house
BAY-43-9695 is a non-nucleoside compound with anti-human cytomegalovirus (HCMV) activity. It is the major metabolite of BAY-38-4766.
  • Inquiry Price
6-8weeks
Size
QTY
TargetMol | Inhibitor Sale
Foscarnet sodium
Phosphonoformate
T022063585-09-1
Foscarnet sodium (Phosphonoformate) is an antiviral agent used in the treatment of cytomegalovirus retinitis. Foscarnet also shows activity against human herpesviruses and HIV.
  • Inquiry Price
Size
QTY
Brivudine
Bromovinyldeoxyuridine, BVDU
T071869304-47-8
Brivudine (BVDU), an antiviral medicine, is used in the therapy of herpes zoster.
  • Inquiry Price
Size
QTY
Ganciclovir sodium
RS-21592 sodium, Cytovene IV sodium, 2'-Nor-2'-deoxyguanosine sodium, BW 759 sodium
T22337107910-75-8
Ganciclovir sodium (Cytovene IV sodium) is the sodium salt of Ganciclovir with antiviral activity, especially against cytomegalovirus (CMV) and herpes simplex virus type 1 (HSV-1).
  • Inquiry Price
Size
QTY
Ca-DTPA trisodium salt hydrate
Calcium trinatrium diethylenetriaminepentaacetic acid hydrate, Ca-DTPA trisodium salt hydrate
T39477207226-35-5
Calcium trinatrium diethylenetriaminepentaacetic acid hydrate (Ca-DTPA trisodium salt hydrate) is a metal chelator and a nontoxic inhibitor of CMV replication, as well as a useful antidote in cases of acute cadmium intoxication.
  • Inquiry Price
Size
QTY
TargetMol | Inhibitor Sale
Cyclopropavir
MBX-400,Filociclovir,ZSM-I-62
T15028632325-71-4In house
Cyclopropavir (Filociclovir; MBX-400) is a compound of broad-spectrum anti-herpesvirus. It has good antiviral activity against cytomegalovirus (CMV), herpes simplex virus (HHV)-6 and HHV-8 (EC50s: 0.7 μM to 8 μM).
  • Inquiry Price
8-10 weeks
Size
QTY
Tricin
TN1068520-32-1
Tricin can inhibit human cytomegalovirus (HCMV) replication by inhibiting CDK9. Tricin inhibits the proliferation and invasion of C6 glioma cells via the upregulation of focal-adhesion-finase (FAK)-targeting microRNA-7.
  • Inquiry Price
Size
QTY
Brincidofovir
CMX001, HDP-CDV
TQ0095444805-28-1
Brincidofovir (HDP-CDV) is an orally active, lipophilic form of cidofovir. It has enhanced activity compared to CDV against certain adenoviruses, herpesviruses, and orthopoxviruses.
  • Inquiry Price
Size
QTY
TargetMol | Inhibitor Sale
Artemisone
BAY 44-9585, Artemifone
T14324255730-18-8
Artemisone (BAY 44-9585) is a potent and semi-synthetic antimalarial, inhibits P. falciparum strains (IC50: 0.83 nM). It also is a potent inhibitor of human CMV.
  • Inquiry Price
Size
QTY
Enocitabine
T1523555726-47-1
Enocitabine is a nucleoside analog. Enocitabine inhibits the replication of human cytomegalovirus(HCMV) and it also has antileukemic and antiviral activities. Enocitabine is also a potent DNA replication inhibitor and a DNA chain terminator.
  • Inquiry Price
4-6 weeks
Size
QTY
CMV-423
RPR-111423
T201513186829-19-6
CMV-423 is an antiviral agent exhibiting effective in vitro activity against beta-herpesviruses, including Human Cytomegalovirus (HCMV), Human Herpesvirus 6 (HHV-6), and Human Herpesvirus 7 (HHV-7). It is utilized in antiviral research.
  • Inquiry Price
10-14 weeks
Size
QTY
Maribavir
Benzimidavir, BW1263W94, GW257406X
T2162176161-24-3
Maribavir (GW257406X) is an orally available benzimidazole riboside compound with activity against cytomegalovirus (CMV). Maribavir is a selective ATP competitor of the viral UL97 kinase, which is involved in viral nuclear maturation events, such as viral DNA assembly and movement of viral capsids from the nucleus of infected cells. Maribavir has activity against strains of CMV that are resistant to standard anti-CMV agents.
  • Inquiry Price
Size
QTY
TargetMol | Inhibitor Sale
SGM8
T28767882268-09-9
SGM8 is a covalent allosteric inhibitor of human cytomegalovirus DNA polymerase subunit Interactions.
  • Inquiry Price
6-8 weeks
Size
QTY
T-611 free base
T-611, T2611, T-2611, T-902611, T-0902611, T0902611
T28905350595-60-7
T-611, a cytomegalovirus replication inhibitor, is used potentially for the treatment of cytomegalovirus infections.
  • Inquiry Price
6-8 weeks
Size
QTY
CC 401 dihydrochloride
T36673
High affinity JNK inhibitor (Ki values are 25-50 nM). Inhibits JNK via competitive binding of the ATP-binding site of active, phosphorylated JNK. Exhibits > 40-fold selectivity for JNK over p38, ERK, IKK2, protein kinase C, Lck and ZAP70. Hepatoprotective. Also inhibits HCMV replication. Uehara et al (2004) c-Jun N-terminal kinase mediates hepatic injury after rat liver transplantation. Transplantation. 78 324 PMID:15316358 |Uehara et al (2005) JNK mediates hepatic ischemia reperfusion injury. J.Hepatol. 42 850 PMID:15885356 |Ma et al (2007) A pathogenic role for c-Jun amino-terminal kinase signaling in renal fibrosis and tubular cell apoptosis. J.Am.Soc.Nephrol. 18 472 PMID:17202416 |Ma et al (2009) Blockade of the c-Jun amino terminal kinase prevents crescent formation and halts established anti-GBM glomerulonephritis in the rat. Lab.Invest. 89 470 PMID:19188913 |Zhang et al (2015) The c-Jun N-terminal kinase inhibitor SP600125 inhibits human cytomegalovirus replication. J.Med.Virol. 87 2135 PMID:26058558 |Vasilevskaya et al (2015) Inhibition of JNK sensitizes hypoxic colon cancer cells to DNA-damaging agents. Clin.Cancer.Res. 21 4143 PMID:26023085
  • Inquiry Price
Size
QTY
PMEDAP
T38514113852-41-8
PMEDAP is a potent inhibitor of Moloney murine sarcoma virus (MSV)-induced tumor formation and mortality, as well as a human immunodeficiency virus (HIV) replication inhibitor with anti-murine cytomegalovirus (MCMV) activity.
  • Inquiry Price
Size
QTY